prazosin hcl

Generic: prazosin hcl

Labeler: direct_rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hcl
Generic Name prazosin hcl
Labeler direct_rx
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 5 mg/1

Manufacturer
Direct_Rx

Identifiers & Regulatory

Product NDC 72189-470
Product ID 72189-470_2c4e047c-e0ff-db6f-e063-6394a90ac37a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215697
Listing Expiration 2026-12-31
Marketing Start 2023-05-11

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189470
Hyphenated Format 72189-470

Supplemental Identifiers

RxCUI
198141
UNII
X0Z7454B90

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name prazosin hcl (source: ndc)
Generic Name prazosin hcl (source: ndc)
Application Number ANDA215697 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 30 CAPSULE in 1 BOTTLE (72189-470-30)
source: ndc

Packages (1)

72189-470-30 30 CAPSULE in 1 BOTTLE (72189-470-30)

Ingredients (1)

prazosin hydrochloride (5 mg/1)

Linked Drug Pages (1)

Prazosin HCL ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2c4e047c-e0ff-db6f-e063-6394a90ac37a", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["fb6db16d-3768-631b-e053-6294a90a1cee"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE (72189-470-30)", "package_ndc": "72189-470-30", "marketing_start_date": "20230511"}], "brand_name": "Prazosin HCL", "product_id": "72189-470_2c4e047c-e0ff-db6f-e063-6394a90ac37a", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "72189-470", "generic_name": "Prazosin HCL", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin HCL", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215697", "marketing_category": "ANDA", "marketing_start_date": "20230511", "listing_expiration_date": "20261231"}